Добірка наукової літератури з теми "Thiocarbonyl Group"
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Статті в журналах з теми "Thiocarbonyl Group"
Kirby, Christopher W., Michael D. Lumsden, and Roderick E. Wasylishen. "A solid-state 13C NMR and theoretical investigation of carbonyl and thiocarbonyl carbon chemical shift tensors." Canadian Journal of Chemistry 73, no. 4 (April 1, 1995): 604–13. http://dx.doi.org/10.1139/v95-078.
Повний текст джерелаMOLINA, M. T., M. YANEZ, O. MO, R. NOTARIO, and J. L. M. ABBOUD. "ChemInform Abstract: The Thiocarbonyl Group." ChemInform 29, no. 13 (June 23, 2010): no. http://dx.doi.org/10.1002/chin.199813281.
Повний текст джерелаFernandez, José Manuel García, and Carmen Ortiz Mellet. "The Thiocarbonyl Group in Carbohydrate Chemistry." Sulfur reports 19, no. 1 (September 1996): 61–159. http://dx.doi.org/10.1080/01961779608047905.
Повний текст джерелаCorsaro, Antonino, and Venerando Pistarà. "Conversion of the thiocarbonyl group into the carbonyl group." Tetrahedron 54, no. 50 (December 1998): 15027–62. http://dx.doi.org/10.1016/s0040-4020(98)00880-1.
Повний текст джерелаCrich, David, and Leticia Quintero. "Radical chemistry associated with the thiocarbonyl group." Chemical Reviews 89, no. 7 (November 1989): 1413–32. http://dx.doi.org/10.1021/cr00097a001.
Повний текст джерелаKook Sohn, Chang, Eun Kyung Ma, Chang Kon Kim, Hai Whang Lee, and Ikchoon Lee. "Theoretical studies on thiocarbonyl group transfer reactions." New Journal of Chemistry 25, no. 6 (2001): 859–63. http://dx.doi.org/10.1039/b010202o.
Повний текст джерелаHuang, Chun-Hao, Pei-Jhen Wu, Kun-You Chung, Yi-An Chen, Elise Y. Li, and Pi-Tai Chou. "Room-temperature phosphorescence from small organic systems containing a thiocarbonyl moiety." Physical Chemistry Chemical Physics 19, no. 13 (2017): 8896–901. http://dx.doi.org/10.1039/c7cp00074j.
Повний текст джерелаAbram, Ulrich, and Bernd Lorenz. "Thiocarbonyl Complexes of Rhenium. Part I." Zeitschrift für Naturforschung B 48, no. 6 (June 1, 1993): 771–77. http://dx.doi.org/10.1515/znb-1993-0611.
Повний текст джерелаBarton, Derek H. R., Peter I. Dalko, and Stephan D. Géro. "Radical cation reactions associated with the thiocarbonyl group." Tetrahedron Letters 33, no. 14 (March 1992): 1883–86. http://dx.doi.org/10.1016/s0040-4039(00)74167-0.
Повний текст джерелаGARCIA FERNANDEZ, J. M., and C. ORTIZ MELLET. "ChemInform Abstract: The Thiocarbonyl Group in Carbohydrate Chemistry." ChemInform 28, no. 28 (August 3, 2010): no. http://dx.doi.org/10.1002/chin.199728234.
Повний текст джерелаДисертації з теми "Thiocarbonyl Group"
Lin, Mei-Huei, and 林浼憓. "A stereoselective glycosylation assisted by using thiocarbonyl as the auxiliary group." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/f37j9b.
Повний текст джерела國立臺灣科技大學
化學工程系
106
Deoxy sugar is a core structure dominating an important role in living organisms. However, the mechanism is still unclear because of low yield and poor selectivity in organic synthesis. To achieve these challenges, a one pot synthetic strategy was established by using phenyl thionocarbonyl group. First, with a single step, the phenoxythiocarbonyl donor, a precursor of deoxy sugar, was obtained in high yield. Secondly, phenoxythiocarbonyl donor was employed to achieve stereoselective glycosylation by using neighboring group participation. Finally, the reaction mechanism was clarified in low temperature NMR experiments, and phenyl thionocarbonyl group was applied to control high -selective glycosylation in wide disaccharide molecules.
CHANG, YA-JOU, and 張雅柔. "The Development of Preactivation Time-Dependent Stereoselective Glycosylation Reaction with 3, 4-Thiocarbonyl Group." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/49z5ju.
Повний текст джерела國立中正大學
化學暨生物化學研究所
108
The carbohydrates play an important role in bio-organism. They not only provide and store energy for daily activities, but also regulate many physiological functions with the others biomolecule on cell surface. To further study the mechanism of carbohydrates in organisms, making a correct stereoselectivity compound during synthesizing is an important work. In the way of organic synthesis, it can be divided to two methods depending on the order of adding activated reagent, one is nonpreactivation, the other is preactivation. The stereoselectivity may be influenced by preactivation time, because the different preactivation time may lead to the different ratio between the kinetic and thermodynamic intermediate. In this thesis,we designed three different functional group donors to study the relationship between preactivation time and stereoselectivity. The results showed that 3, 4-carbonyl and 3, 4-thiocarbonyl donor have the opposite trends of stereoselectivity with different preactivation time. Based on the experimental result, it could be suggested that the intermediate may affect the stereoselectivity. On the other hand, when different acceptors was glycosylated by 3, 4-thiocarbonyl galactoside with the different preactivation time, we could get various trends of stereoselectivity. According to this trends, acceptors could be classified to three types: high reactivity organic small molecule, high reactivity carbohydrate and poor reactivity carbohydrate.
Частини книг з теми "Thiocarbonyl Group"
Sato, S., and N. Furukawa. "Thiocarbonyl as Functional Group." In Four Carbon-Heteroatom Bonds, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-018-01031.
Повний текст джерелаManyem, S., and M. P. Sibi. "Intramolecular Transfer of Sulfur from a Thiocarbonyl Group." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00531.
Повний текст джерелаBarluenga, José, Eduardo Rubio, and Miguel Tomás. "Functions Containing a Thiocarbonyl Group Bearing Two Heteroatoms Other Than a Halogen or Chalcogen." In Comprehensive Organic Functional Group Transformations, 569–85. Elsevier, 1995. http://dx.doi.org/10.1016/b0-08-044705-8/00228-4.
Повний текст джерелаBarluenga, J., E. Rubio, and M. Tomás. "Functions Containing a Thiocarbonyl Group Bearing Two Heteroatoms Other Than a Halogen or Chalcogen." In Comprehensive Organic Functional Group Transformations II, 545–72. Elsevier, 2005. http://dx.doi.org/10.1016/b0-08-044655-8/00139-2.
Повний текст джерелаKleinpeter, Erich, and Kalevi Pihlaja. "Functions Containing a Thiocarbonyl Group and at Least One Halogen; Also at Least One Chalcogen and No Halogen." In Comprehensive Organic Functional Group Transformations, 527–67. Elsevier, 1995. http://dx.doi.org/10.1016/b0-08-044705-8/00273-9.
Повний текст джерелаKleinpeter, E. "Functions Containing a Thiocarbonyl Group and at Least One Halogen; Also at Least One Chalcogen and No Halogen." In Comprehensive Organic Functional Group Transformations II, 495–544. Elsevier, 2005. http://dx.doi.org/10.1016/b0-08-044655-8/00138-0.
Повний текст джерелаKantlehner, W. "Transformation of Carbonyl or Thiocarbonyl Groups into Methylene Groups." In Three Carbon-Heteroatom Bonds: Amides and Derivatives; Peptides; Lactams, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-022-00951.
Повний текст джерелаWakefield, Basil J. "Carbophilic Addition of Organomagnesium Compounds to Thiocarbonyl Groups." In Organomagnesium Methods in Organic Synthesis, 147–50. Elsevier, 1995. http://dx.doi.org/10.1016/b978-012730945-3.50009-8.
Повний текст джерелаTracey, M. R., R. P. Hsung, J. Antoline, K. C. M. Kurtz, L. Shen, B. W. Slafer, and Y. Zhang. "Tungsten(0)-Mediated Coupling of Thiocarbonyl and Thioacetal Groups." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00392.
Повний текст джерелаHall, D. G., and H. Zheng. "Addition of Diboron Species to Carbonyl or Thiocarbonyl Groups, or Aldimines." In Boron Compounds, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-106-00011.
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